EXPRESSION OF MITOTIC CYCLIN B1 IS NOT CONFINED TO PROLIFERATING CELLS IN THE RAT TESTIS

Citation
J. Gromoll et al., EXPRESSION OF MITOTIC CYCLIN B1 IS NOT CONFINED TO PROLIFERATING CELLS IN THE RAT TESTIS, Biology of reproduction, 57(6), 1997, pp. 1312-1319
Citations number
28
Journal title
ISSN journal
00063363
Volume
57
Issue
6
Year of publication
1997
Pages
1312 - 1319
Database
ISI
SICI code
0006-3363(1997)57:6<1312:EOMCBI>2.0.ZU;2-G
Abstract
Spermatogenesis is a precisely controlled and timed process comprising mitotic divisions of spermatogonia, meiotic divisions of spermatocyte s, and the maturation and differentiation of haploid spermatids. Cell proliferation is controlled by genes involved in the regulation of the cell cycle. Among the principal regulatory proteins are cyclins, whic h are categorized according to their appearance during the cell cycle. B-type cyclins are mitotic cyclins and function at the G2/M transitio n of the cell cycle. We have investigated the expression and regulatio n of cyclin B1 during rat spermatogenesis. Rat cyclin B1 was isolated from a testis cDNA library and further used as a probe to detect mRNA expression. Northern blot hybridization of testis mRNA revealed the pr esence of a single 1.7-kilobase transcript. In situ hybridization show ed stage-specific expression during spermatogenesis with highest expre ssion found in late pachytene spermatocytes and early round spermatids . This pattern was confirmed in fractions of isolated germ cells. Immu nocytochemistry displayed highest protein levels in round spermatids. Depletion of gonadotropins did not change the quantitative and qualita tive expression pattern of cyclin B1. Therefore, the signals triggerin g the onset of cyclin B1 expression seem not to originate from the pit uitary-gonadal endocrine axis and might therefore be paracrine factors originating within the germinal epithelium. Our observations suggest that cyclin B1 plays a hitherto unknown role in spermatid maturation i n addition to its known function in dividing cells.